Multiple synostoses syndrome 3
MONDO:0013064Any multiple synostoses syndrome in which the cause of the disease is a mutation in the FGF9 gene.
Also known as: FGF9 multiple synostoses syndrome, multiple synostoses syndrome 3, multiple synostoses syndrome caused by mutation in FGF9, multiple synostoses syndrome type 3, SYNS3
1 clinical trial for this condition and its sub-types, 0 tagged with Multiple synostoses syndrome 3 itself.
Follow this condition to get notified about new trials